Double-Blind, Placebo-Controlled Study of E-B-FAHF-2 in Combination With Omalizumab-Facilitated Multiallergen Oral Immunotherapy

被引:9
作者
Wang, Julie [1 ,8 ]
Wood, Robert A. [2 ]
Raymond, Samantha [3 ]
Suarez-Farinas, Mayte [3 ,4 ]
Yang, Nan [5 ,6 ]
Sicherer, Scott H. [1 ]
Sampson, Hugh A. [1 ]
Li, Xiu-Min [6 ,7 ]
机构
[1] Jaffe Food Allergy Inst, Icahn Sch Med Mt Sinai, New York, NY USA
[2] Johns Hopkins Univ, Sch Med, Dept Pediat, Baltimore, MD USA
[3] Icahn Sch Med Mt Sinai, Dept Populat Hlth Sci & Policy, New York, NY USA
[4] Icahn Sch Med Mt Sinai, Dept Genet & Genom Sci, New York, NY USA
[5] Gen Nutraceut Technol, Elmsford, NY USA
[6] New York Med Coll, Dept Pathol Microbiol & Immunol, Valhalla, NY USA
[7] New York Med Coll, Dept Otolaryngol, Valhalla, NY USA
[8] Jaffe Food Allergy Inst, Icahn Sch Med Mt Sinai, Dept Pediat, Div Allergy & Immunol, 1 Gustave L Levy Pl, POB 1198, New York, NY 10029 USA
关键词
Chinese herbal therapy; E-B-FAHF-2; Desensitization; Food allergy; Peanut allergy; Remission; ALLERGY HERBAL FORMULA-2; FOOD ALLERGY; IMMUNOLOGICAL ACTIONS; MURINE MODEL; COWS MILK; SAFETY; EFFICACY; DESENSITIZATION; CHILDREN; FAHF-2;
D O I
10.1016/j.jaip.2023.03.051
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
BACKGROUND: Oral immunotherapy (OIT) is limited by adverse events, and most patients require continued treatment to maintain their increased threshold. Adjunctive treatments have been explored to increase the safety and efficacy of OIT.OBJECTIVE: This study aimed to determine the safety and efficacy of enhanced, butanol purified Food Allergy Herbal Formula-2 (E-B-FAHF-2) for inducing remission in subjects undergoing omalizumab-facilitated multiallergen OIT (multi -OIT).METHODS: In this double-blind, placebo-controlled clinical trial, subjects were randomized 1:1 to receive either E-B-FAHF-2 or placebo, starting 2 months before OIT and continuing throughout OIT. All subjects received a 4-month course of omalizumab, starting 2 months before OIT through the 2 -month OIT build-up phase. After 24 months of multi-OIT (maintenance dose of 1000 mg of each allergen), desensitization and remission were assessed. The primary objective was to determine if subjects in the E-B-FAHF-2 group (EOIT) were more likely than the placebo group (OIT) to develop remission to all 3 allergens treated with multi-OIT, as defined by the absence of dose-limiting symptoms to a cumulative dose of 4444 mg of protein after discontinuing treatment for 3 months. RESULTS: Thirty-three subjects were randomized. A total of 63.6% were desensitized to 4444 mg of protein for each allergen at 26 months, and 24.2% met the primary outcome of remission at 29 months, with no difference between the treatment groups. There was good adherence (>85%) with study medications, with no difference between the treatment groups. There was no difference in reported overall adverse events between the treatment groups. CONCLUSION: Omalizumab-facilitated multifood OIT was safe and effective, and remission was achieved in about a quarter of subjects. However, outcomes were not improved by the addition of E-B-FAHF-2. & COPY; 2023 American Academy of Allergy, Asthma & Immunology (J Allergy Clin Immunol Pract 2023;11:2208-16)
引用
收藏
页码:2208 / 2216.e1
页数:10
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